Iyi mifananidzo yevana vane Down's syndrome inoshandura maonero ako nezvehurema uhu

Trisomy 21: vana vanomira pasi pe lenzi yaJulie Willson

“Ndiri mumwe wevanhu vane rombo rakanaka vakakura nehanzvadzi yaiva neDown’s syndrome. Dina akanga ari chinhu chakanakisisa chingave chakaitika kumhuri yedu. Akatidzidzisa kuti rudo rwechokwadi rusina magumo chii uye mafambiro ehupenyu pasina kunetseka. Dina akafa nekushaya simba kwemoyo pazera remakore 21 apo tarisiro yeupenyu yake haina kupfuura zera remakore 35. Ndizvo nemashoko aya apo Julie Willson, mutori wemifananidzo wechidiki weAmerica, akarumbidza hanzvadzi yake papeji yake yeFacebook. Kubva achitanga kutora mafoto, Julie Willson agara achida kutora mifananidzo vana vane Down syndrome.. Nhasi ari kutsikisa nhevedzano yakaisvonaka yemifananidzo kuratidza runako nomufaro weava vana vakasiyana uye pamusoro pezvose kuita kuti nhamba hurusa izive nezvehurema uhu husingadzivisiki. “Ndinoda kuchinja pfungwa. Ratidza vabereki vari kugadzirira kugamuchira mwana ane Down's syndrome kuti hapana chakanyanya kunaka uye kuti vachakomborerwa. Kana iwe uri munhu uya ari kuenda ku "emotional roller coaster" nekuti mwana wako ane Down syndrome, ziva kuti wave kuda kusangana nerudo runopfuura zvese zvaunotarisira. ”

Verenga zvakare: Down syndrome: amai vanotora kasikana kavo semwanasikana chaiye weDisney